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Synergetics 65935

by Synergetics USA, Inc.

Synergetics 65935 is a vitrectomy system micro-cutting unit (FDA Class II; FDA product code HQE, Instrument, vitreous aspiration and cutting, ac-powered) made by Synergetics USA, Inc., listed in FDA GUDID since 20 Sep 2016 (UDI-DI 20841305110599), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number20841305110599 UDI-DI Date20 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Synergetics
Generic name
Vitrectomy system micro-cutting unit
Model / Ref / Catalog
65935
Primary DI / UDI-DI
20841305110599
FDA product code
HQE
GMDN term
Vitrectomy system micro-cutting unit
Device class
Class II
Regulation number
886.4150
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vitrectomy system micro-cutting unit

Similar devices

Other devices filed under FDA product code HQE (Instrument, vitreous aspiration and cutting, ac-powered).

Other devices from Synergetics, Inc.

See all devices from Synergetics, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)